Disease: Night Blindness, Congenital Stationary, Autosomal Dominant 3 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs786205853
rs786205853
Entrez Id: 2779
Gene Symbol: GNAT1
GNAT1
CUI: C1864870
Disease:
Night Blindness, Congenital Stationary, Autosomal Dominant 3 		0.800 GeneticVariation UNIPROT
dbSNP: rs786205853
rs786205853
Entrez Id: 2779
Gene Symbol: GNAT1
GNAT1
CUI: C1864870
Disease:
Night Blindness, Congenital Stationary, Autosomal Dominant 3 		G 0.800 CausalMutation CLINVAR